EGFR c.707G>T ;(p.C236F)

Variant ID: 7-55220317-G-T

NM_005228.3(EGFR):c.707G>T;(p.C236F)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of pathogenic missense mutations using protein stability predictors.

Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21

Variant appearance in text: EGFR: C236F
PubMed Link: 32958805
Variant Present in the following documents:
  • 41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page



Advances in dynamic modeling of colorectal cancer signaling-network regions, a path toward targeted therapies.

Oncotarget
Tortolina, Lorenzo L; Duffy, David J DJ; Maffei, Massimo M; Castagnino, Nicoletta N; Carmody, Aimée M AM; Kolch, Walter W; Kholodenko, Boris N BN; De Ambrosi, Cristina C; Barla, Annalisa A; Biganzoli, Elia M EM; Nencioni, Alessio A; Patrone, Franco F; Ballestrero, Alberto A; Zoppoli, Gabriele G; Verri, Alessandro A; Parodi, Silvio S
Publication Date: 2015-03-10

Variant appearance in text: EGFR: c236f
PubMed Link: 25671297
Variant Present in the following documents:
  • oncotarget-06-5041-s001.pdf
View BVdb publication page



Mutant p53 in cancer: new functions and therapeutic opportunities.

Cancer Cell
Muller, Patricia A J PA; Vousden, Karen H KH
Publication Date: 2014-03-17

Variant appearance in text: EGFR: C236F
PubMed Link: 24651012
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page